DOID:0111153 - congenital mirror movement disorder
Disease Ontology Definition:A movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs.
Synonyms: familial congenital controlateral synkinesia, familial congenital mirror movements, hereditary congenital controlateral synkinesia, hereditary congenital mirror movements, isolated congenital controlateral synkinesia, isolated congenital mirror movements
|MONDO:0016558 - familial congenital mirror movements|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : dcc, dnal4, ntn1, rad51
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD